Canonical Allele Identifier: PA2826034902
Gene: PFKM HGNC NCBI
ClinVar RCV:
RCV000001216
ClinVar Variation:
1157
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001160160.1:p.Arg39Leu
CA114804
NM_001166688.2:c.116G>T